TruVision Health LLC

Recall #F-0942-2023 · Initiated 2023-04-27

Product

reFORM

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

Quantity affected

2,535 packs

Distribution

Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand

Lot / code info

Lot 34159

Voluntary / mandated

Voluntary: Firm initiated

Initial notification

Press Release